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Intrafamilial neurological phenotypic variability due to either biallelic or monoallelic pathogenic variants in CACNA1A.
Published in:
Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1458109
By:
- Mammadova, Dilbar;
- Kraus, Cornelia;
- Leis, Thomas;
- Popp, Bernt;
- Zweier, Christiane;
- Reis, Andre;
- Trollmann, Regina
Publication type:
Article
Intrafamilial neurological phenotypic variability due to either biallelic or monoallelic pathogenic variants in CACNA1A.
Published in:
Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1458109
By:
- Mammadova, Dilbar;
- Kraus, Cornelia;
- Leis, Thomas;
- Popp, Bernt;
- Zweier, Christiane;
- Reis, Andre;
- Trollmann, Regina
Publication type:
Article
HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders.
Published in:
American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3162, doi. 10.1002/ajmg.a.36766
By:
- Reuter, Miriam S.;
- Sass, Jörn Oliver;
- Leis, Thomas;
- Köhler, Julia;
- Mayr, Johannes A.;
- Feichtinger, RENé G.;
- Rauh, Manfred;
- Schanze, Ina;
- Bähr, Luzy;
- Trollmann, Regina;
- Uebe, SteffEN;
- Ekici, Arif B.;
- Reis, André
Publication type:
Article
Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL.
Published in:
Oncogene, 2001, v. 20, n. 23, p. 2900, doi. 10.1038/sj.onc.1204401
By:
- Reichel, Martin;
- Gillert, Esther;
- Angermüller, Sieglinde;
- Hensel, Jan Patrick;
- Heidel, Florian;
- Lode, Martin;
- Leis, Thomas;
- Biondi, Andrea;
- Haas, Oskar A;
- Strehl, Sabine;
- Panzer-Grümayer, E Renate;
- Griesinger, Frank;
- Beck, Jörn D;
- Greil, Johann;
- Fey, Georg H;
- Uckun, Fatih M;
- Marschalek, Rolf
Publication type:
Article
A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells.
Published in:
Oncogene, 1999, v. 18, n. 33, p. 4663, doi. 10.1038/sj.onc.1202842
By:
- Gillert, Esther;
- Leis, Thomas;
- Repp, Reinald;
- Reichel, Martin;
- Hösch, Annette;
- Breitenlohner, Ina;
- Angermüller, Sieglinde;
- Borkhardt, Arndt;
- Harbott, Jochen;
- Lampert, Fritz;
- Griesinger, Frank;
- Greil, Johann;
- Fey, Georg H;
- Marschalek, Rolf
Publication type:
Article
Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23).
Published in:
Oncogene, 1997, v. 14, n. 2, p. 195, doi. 10.1038/sj.onc.1200814
By:
- Borkhardt, Arndt;
- Repp, Reinald;
- Haas, Oskar A;
- Leis, Thomas;
- Harbott, Jochen;
- Kreuder, Joachim;
- Hammermann, Jutta;
- Henn, Traudl;
- Lampert, Fritz
Publication type:
Article
Drug utilisation on a preterm and neonatal intensive care unit in Germany: a prospective, cohort-based analysis.
Published in:
European Journal of Clinical Pharmacology, 2010, v. 66, n. 1, p. 87, doi. 10.1007/s00228-009-0722-8
By:
- Neubert, Antje;
- Lukas, Kristin;
- Leis, Thomas;
- Dormann, Harald;
- Brune, Kay;
- Rascher, Wolfgang
Publication type:
Article
Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: Almost identical MLL breakpoints in therapy-related AML after treatment without etoposides.
Published in:
Genes, Chromosomes & Cancer, 2003, v. 36, n. 4, p. 393, doi. 10.1002/gcc.10167
By:
- Thorsten Langer;
- Markus Metzler;
- Dirk Reinhardt;
- Susanne Viehmann;
- Arndt Borkhardt;
- Martin Reichel;
- Martin Stanulla;
- Martin Schrappe;
- Ursula Creutzig;
- Jörg Ritter;
- Thomas Leis;
- Ulla Jacobs;
- Jochen Harbott;
- Jörn D. Beck;
- Wolfgang Rascher;
- Reinald Repp
Publication type:
Article

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